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TPM3 mutation in one of t… - University of Gothenburg, Sweden Till startsida
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TPM3 mutation in one of the original cases of cap disease.

Journal article
Authors Monica Ohlsson
Anna Fidzianska
Homa Tajsharghi
Anders Oldfors
Published in Neurology
Volume 72
Issue 22
Pages 1961-3
ISSN 0028-3878
Publication year 2009
Published at Institute of Biomedicine, Department of Pathology
Pages 1961-3
Language en
Keywords Adult, Age of Onset, Amino Acid Substitution, genetics, Craniofacial Abnormalities, genetics, DNA Mutational Analysis, Disease Progression, Female, Genetic Markers, genetics, Genetic Predisposition to Disease, genetics, Humans, Muscle Weakness, genetics, physiopathology, Muscle, Skeletal, metabolism, pathology, physiopathology, Muscular Diseases, diagnosis, genetics, physiopathology, Mutation, genetics, Mutation, Missense, genetics, Pneumonia, etiology, Respiration, Artificial, Respiratory Paralysis, complications, physiopathology, Spinal Curvatures, etiology, Tropomyosin, genetics
Subject categories Cell and Molecular Biology
Page Manager: Webmaster|Last update: 9/11/2012

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